Therapeutically countoured, compliance encouraging aligner implement

ABSTRACT

Described is an orthodontic aligner implement that can ensure the accuracy and efficiency of clear aligner orthodontic therapies as well as increase patient compliance by reducing discomfort and combining functionality into a breath-freshening medium. The implement includes a consumable mass having at least two channels disposed on opposite sides of the mass and traversing the width of the mass. The channels are adapted to seat between opposing anterior or incisor teeth. Also described is a method of positioning an orthodontic aligner into a prescribed position that includes placing the aligner approximately in the prescribed position in one&#39;s mouth, placing the aligner implement described above into the mouth, and applying the implement in contact with the aligner in one&#39;s mouth.

CROSS REFERENCE TO RELATED APPLICATION

This application claims priority to U.S. Provisional Patent ApplicationNo. 61/877,656 filed Sep. 13, 2013, the entire contents of which areherein incorporated by reference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The invention relates to a method of and device for ensuring theaccuracy and efficiency of clear aligner orthodontic therapies as wellas increasing patient compliance by reducing discomfort and combiningfunctionality into a breath-freshening medium.

2. Description of Related Art

“Clear aligner therapy” can be defined as any treatment which relies onthe continuous wearing of a clear plastic shell, or template, whichcorresponds to a specific alignment of the dentition that does not quitematch the wearer's current alignment, in an effort to improve dentalalignment. There are multiple custom fabricated clear aligner therapiesavailable to clinicians. Examples of these include, but are not limitedto, Invisalign®, ClearCorrect™, Simpli5™, etc. These therapies are“custom fabricated” because of the precision technology that goes intocreating a sequence of aligners which are capable of guiding theprogression of alignment in a desirable manner. Clear aligner therapyincludes treatment for an individual who recently completed orthodontictherapy of any kind and has been given an Essix® retainer to prevent“relapse.” Essix® retainers are clear plastic shells, provided afterbraces are removed in order to maintain alignment and occlusalcorrection post-treatment. “Relapse” refers to any movement of thedentition in a direction away from ideal alignment and usually towardsthe individual's original malocclusion; this is usually a result ofnon-compliance with wearing the prescribed retainer. Any relapse of thedentition's alignment will prevent the template from seating fully onthe teeth. However, until complete loss of fit occurs, it is sometimespossible to recapture the alignment corresponding to the template withfull time wear and some chewing exercises. If this is the prescribedcourse of treatment, the retainer then becomes a clear aligner.

The processes which can re-align a relapsed dentition are the same asthose employed in the previously mentioned clear aligner therapies. Evenwith recent technological advances in the fabrication of the sequence ofaligners, the success of these therapies, much like an attempt atre-alignment via the use of an Essix® retainer, is almost purely relianton patient cooperation and compliance with the prescribed treatmentregimen. Common compliance issues are due to inconvenience, soreness,and bad breath. When compliance is lacking, the first given sequence ofaligners is rarely enough to achieve the desired alignment, and theresult is a loss of “tracking” somewhere within the given sequence ofaligners. Tracking refers to the ability of the given sequence ofaligners to keep pace with the simulated and prescribed tooth movement.Any inequity of the computer simulation to the biology and capacity ofthe individual's teeth to move at the prescribed rate may cause a lossof tracking; or, as previously stated, a simple lack of wearing thealigners as prescribed may also result in a loss of tracking. Even ifpatient compliance is exemplary, sometimes a loss of tracking will occurif the computer simulation is somehow not reflective of the actualbiology and/or ability of the individual's teeth to move at the expected(prescribed) rate. It is sometimes possible to recapture desiredtracking by extending the wear time of the aligner which displays thepoor tracking; however, without an implement to augment the action ofthe poorly tracking aligner, it is rarely successful.

When a loss of tracking occurs to the extent that the remaining unusedaligners are unusable, using the Invisalign® system as an example, a“refinement” is ordered. A refinement is a new sequence of alignersdelivered with the starting point being the current and improvedalignment (the result of the first sequence of aligners given up untilthey no longer were effective) and an end point typically consistentwith the originally prescribed end point. Three refinements are includedin the initial lab fee paid for by the treating doctor. It is sometimesnecessary to exhaust these refinements to satisfy a patient'sexpectations. The combination of additional refinements and a lengthy,unanticipated treatment time is extremely costly. My use of the terms“clear aligner therapy” and “aligner therapy” is intended also toinclude such additional refinements involving a new sequence ofaligners. The inventor is not aware of aligners that are other thanclear, but it is possible that colored aligners may at some point beoffered. The applicability of my invention would of course not beaffected by a colored, translucent, or opaque aligner and therefore Iintend for the definition of “aligner” and “clear aligner” as usedherein to include such possible variants.

The typical course of treatment for any clear aligner is for full timewear, except while eating and brushing (or around 22 hours per day asindicated on the Invisalign® website). Advice is given to brush aftereach meal before placing aligners back onto the teeth. It is not alwaysfeasible to follow this advice, and even if it were, food and odorsremain in the mouth even after thorough brushing and flossing.

It would be in the best interest of both the treating doctor and thepatient to have an auxiliary apparatus which could, with proper use,decrease treatment times and improve patient satisfaction and clinicaloutcomes. Another advantageous feature of such an apparatus would beseamless integration into the lifestyle of the individual using it, asthis would promote compliance. Until now, a few of the available optionsfor such an apparatus included “Chewies™” and “Acceledent®”. “Chewies™”are rubberized cotton rolls which are intended to seat aligners up overthe dentition in order to ensure proper fit and “action.” “Action”refers to the flexing of an aligner over the dentition, creating theintended forces necessary for tooth movement into the intendedalignment. The use of “Chewies™” is widely prescribed within theorthodontic and general dental profession when clear aligner therapy isprovided. “Continued action” is action repeated over extended periods oftime.

Moreover, the purpose and necessity of “Chewies” is often lost on apatient because of the foreign nature of the rubbery cotton roll. It isalso lost on treating doctors due to expense and an often justifiedskepticism that the patient will use them. Aligner wearers as well asadolescents wearing Essix® retainers often report bad breath as a reasonfor non-compliance during the day while they are either at work orschool. Furthermore, custom fabricated clear aligner therapies are mostappealing due their ability to blend into everyday life. This is notoften possible for business professionals, students, or anybody wholeads a social and active lifestyle. Thus the orthodontist must addressmotivation and social relationships from the patient's perspective aspart of his or her prescribed treatment.

Acceledent® is a technology which is based on a great deal of researchto prove that vibratory action on the dentition during tooth movementcan have an acceleratory effect. It consists of a horseshoe shaped archmade of rubber which is connected to an apparatus that sends a vibratingcurrent through the rubber arch. When placed in the mouth between thetop and bottom teeth, for 20 minutes daily, treatment times are reportedto decrease by ˜50%. The problem with Acceledent® is that it is oftencost-prohibitive.

Conventional breath freshening implements are not suitable for useduring aligner therapy. Many have convexities to them which often causethem to slip out from within the teeth. Others are flat and, due to the“teetering” effect of a flat object between two opposing points ofcontact, apply laterally-focused forces onto the aligners instead ofvertical “seating” forces. Seating of an aligner refers to thecompression of the aligner onto the teeth which is often what appliesthe prescribed directional forces. Salivary lubrication can also causethem to slip out while attempting to keep them between the teeth. Theseshortcomings are magnified when aligners are worn due to the smooth androunded nature of their exterior.

Continued action is difficult to attain with contemporary availabletherapies. It would be beneficial to all parties involved to have animplement that would promote patient compliance as well as effect toothmovement in a manner aspired to by “Chewies” and Acceledent®, therebyreducing patient and clinician's costs, and improving results andpatient satisfaction. The implement for doing so will be embodied by theinvention described hereinafter.

SUMMARY OF THE INVENTION

The present invention offers an improved device and method by whichclinicians providing, and individuals undergoing, clear aligner therapy(as previously defined) can ensure improved compliance and outcomes. Thepresent invention is particularly advantageous due to the need forcontinued action (as previously defined) of the aligners over the teethin order to achieve timely and predictable results.

The invention comprises a multi-concave implement that preferablycontains xylitol and flavoring for placement in the mouth, to be usedrepeatedly to seat a clear aligner and provide a continuity ofdetermined nudging, or action, of the aligner onto the dentition. Thesethree distinct characteristics of the implement are further describedbelow.

The multi-concave structure of the implement, characterized by at leastone and preferably two sets of opposing grooves or channels, provides aquickly understood incentive for the patient to place it between his orher teeth and work it. The therapy is not only readily adopted, but theimplement is easy to maintain in the proper position, therebyencouraging its use. The concavities act as guidance for the incisorteeth to reproducibly find a comfortable resting spot without muchmental focus or thinking about what is being done. Furthermore, theimplement can be specifically designed to fit comfortably between theteeth in a variety of orientations.

In a preferred embodiment of the invention, each aligner implementcontains at least 0.5 gram xylitol. Xylitol is a sugar alcohol, likesorbitol; both are common refined sugar substitutes, cannot bemetabolized by oral bacteria, and are the science behind the claim“sugarfree” or “sugarless”. Furthermore, xylitol has been proven toinhibit cavity-causing bacteria (S. Mutans) from forming acid. It isoften prescribed (in lozenge or gum form) to high-risk individualsduring preventive and maintenance therapy as well as orthodontic therapyin an effort to avoid decalcification of the dentition. Sorbitol, aswell as synthetic sweeteners, may be substituted. Any sugar substitute,or a mixture of sugar substitutes, which cannot be metabolized by oralbacteria may be used, but xylitol is preferred.

The breath freshening quality of mint has long been available to thepublic and has been a staple in any number of stores and in the media.Mint can include other variations of mint, such as spearmint andpeppermint. It is this familiarity and prevalence in society that willenable it to be readily accepted by patients. In recent years, manyother flavors have been developed for the freshening of one's breath.The implement described herein may use these other flavors as well,which include, but are not limited to, fruit flavorings and cinnamon.For many if not most patients, the entire experience of clear alignertherapy seems strange or unnatural if not grossly intrusive, andaccordingly a pleasant or at least familiar feature such as mintflavoring greatly enhances acceptability. The edible quality of a mintor other flavored implement makes it an ideal vehicle to deliver bothenjoyment and functionality. Combinations of the above-mentioned flavorsmay also be used.

The protective aspect of the implement is something that directlycorrelates to the mission statements of custom fabricated clear alignertherapies: the ability to maintain proper hygiene and dental health dueto the ability to remove the aligners at any time.

The multi-functionality of the invention is one characteristic thatmakes it truly unique. To be able to freshen one's breath, protect one'steeth, and at the same time improve upon treatment duration, patientcomfort, and outcome is something that no other auxiliary to clearaligner therapy can claim.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a front elevation view of an implement according to a firstembodiment of the invention.

FIG. 2 is a rear elevation view of the implement of FIG. 1.

FIG. 3 is a top plan view of the implement of FIG. 1.

FIG. 4 is a bottom plan view of the implement of FIG. 2.

FIG. 5 is a left side elevation view of the implement of FIG. 1.

FIG. 6 is a right side elevation view of the implement of FIG. 1.

FIG. 7 is a perspective view of the implement of FIG. 1.

FIG. 8 is a top plan view of an implement according to a secondembodiment of the invention.

FIG. 9 is a side sectional view of the implement of FIG. 1 in a typicalposition in a patient's mouth.

FIG. 10 is a side sectional view of the implement of FIG. 8 in a typicalposition in a patient's mouth.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

As used herein, spatial or directional terms, such as “left,” “right,”“above,” “below,” “top,” “bottom,” and the like, relate to the implementas it is shown in FIG. 1 unless otherwise noted. However, it is to beunderstood that the implement may assume various alternativeorientations and, accordingly, such terms are not to be considered aslimiting. Further, as used herein, all numbers expressing dimensions,physical characteristics, and the like, used in the specification andclaims are to be understood as being modified in all instances by theterm “about.”

Referring now to FIGS. 1-7, a first embodiment of implement 1 is shown.Implement 1 is preferably a one-piece construction having a lengthdimension L, a height dimension H, and a width dimension W. The ratio ofthe length dimension L to the height dimension H can be 1:1 or near 1:1,in which case implement 1 has a generally square cross-section takenalong line A-A of FIG. 1. Implement 1 also includes a plurality ofconcave channels 2 a-d extending across the width dimension W, andpreferably across the entire width dimension W. Channels 2 a-d aregenerally provided in sets of two with each channel 2 a-d in the setdisposed on an opposite side of implement 1 from the other channel 2 a-dof the set such that each channel 2 a-d in the set can be used to engagewith either the top or bottom teeth of a patient, as described furtherherein. For example, implement 1 can include a top channel 2 a disposedon a top surface 4 of implement 1 and extending across the widthdimension W and a bottom channel 2 b disposed on a bottom surface 5 ofimplement 1 which is opposite top channel 2 a in the height dimension H.Bottom channel 2 b also extends across the width dimension W, andpreferably across the entire width dimension W, of implement 1 and isgenerally parallel to top channel 2 a. Top channel 2 a and bottomchannel 2 b may be slightly offset with respect to one another in thelength dimension L. In other words, bottom channel 2 b may not bedirectly below top channel 2 a, though it is generally positioned belowtop channel 2 a. However, in some non-limiting embodiments, bottomchannel 2 b is directly below top channel 2 a.

Implement 1 can include other channels 2 c-d, preferably provided inoppositely-disposed sets of two, as well. For example, each of left andright side surfaces 6, 7 of implement 1 can include a concave channel 2c-d that extends across the width dimension W, and possibly across theentire width dimension W. Left side channel 2 c on left side surface 6is generally disposed opposite right side channel 2 d on right sidesurface 7 in the length dimension L, though they can be offset from oneanother. As shown in FIG. 1, left side channel 2 c is slightly belowright side channel 2 d in the height dimension H. Offsetting of thechannels 2 a-d can create the “N” or “Z” (depending on the orientation)shape of the implement 1 depicted in FIG. 1. Preferably, the sidesurface channels 2 c, 2 d are smaller and less deep than top and bottomchannels 2 a, 2 b, for reasons that will become apparent below.Additional channels can be provided as well, though the preferredarrangement involves two sets of channels (for a total of four) asdepicted in FIG. 1.

Implement 1 can also include a plurality, and preferably four,protrusions or arms 3 a-3 d, with each disposed at a respective one ofthe corners of implement 1 and extending in the width dimension W ofimplement 1, and preferably across the entire width dimension W. InFIGS. 1-7, each protrusion is depicted as an elongate,smoothly-curvatured member integral with the remainder of implement 1and generally located at a corner of implement 1. In this embodiment,each channel 2 a-d is formed between two protrusions 3 a-d. In otherwords, with reference to FIG. 1, if one were to trace the perimeter ofimplement 1, one would encounter channel 2 a, protrusion 3 b, channel 2d, protrusion 3 c, etc. Implement 1 is not intended to be limited toonly the arrangement shown in FIG. 1 which includes four protrusions 3a-d, though the number of protrusions generally corresponds to thenumber of channels. Thus, by way of example, if implement 1 is designedwith six channels, implement may also include six protrusions with eachchannel being formed between two protrusions.

The shape of protrusions 3 a-d can vary with respect to one another,meaning that, within the same implement 1, there can exist protrusionsof multiple shapes and/or sizes. With reference to FIGS. 1-7, depictedare four protrusions 3 a-d, with two protrusions 3 a, 3 c having thesame first shape and two protrusions 3 b, 3 d having the same secondshape, where the first and second shapes differ from one another. Withreference to FIG. 1, the first and second shapes alternate in theclockwise direction such that the top left protrusion 3 a and bottomright protrusion 3 c are similarly shaped while the top right protrusion3 b and bottom left protrusion 3 d are similarly shaped. In other words,if one were to trace the perimeter of implement 1 in the clockwisedirection, one would encounter protrusion 3 a of a first shape,protrusion 3 b of a second shape, protrusion 3 c of the first shape, andthen protrusion 3 d of the second shape. With this configuration, theview of implement 1 depicted in FIG. 1 would remain unchanged if theimplement 1 were rotated 180° about an axis that passes throughimplement 1 in the width dimension W. With reference to FIG. 1, it canalso be said that if the implement 1 is divided in half along an axispassing through implement 1 in the height dimension H, the left side isan inverted equal of the right side. This symmetry can help ensure thateach side of implement 1 dissolves evenly during use and thus remainshighly functional throughout use.

Some possible, non-limiting dimensions of implement 1 of this embodimentare: Overall length, i.e., the length dimension L, can be betweenapproximately 8 and 12 mm, such as between 10.5 and 11.5 mm. Overallheight, i.e. the height dimension H, can be between 8 and 13 mm, such asbetween 11 and 12.5 mm. As mentioned above, the ratio of lengthdimension L to height dimension H (L:H) is generally near 1:1, such asbetween 0.8:1 and 1.1:1. Overall width, i.e. the width dimension W, canbe between approximately 8 and 13 mm, such as between 10.5 and 12 mm.The length of top and bottom channels 2 a, 2 b, which extend in thewidth dimension W, can be between approximately 8 and 13 mm, such asbetween 11 and 12 mm. The space between the peaks of protrusions 3 a and3 b, and likewise between the peaks of protrusions 3 c and 3 d, can bebetween approximately 5 and 8 mm, such as between 6.5 and 8 mm. Thechannels 2 a-d should be sufficiently wide to accommodate a patient'stooth while still allowing sufficient room for the tooth to be slid backand forth along the arch of channel 2 a-d to work the implement 1. Theaverage front to back width of an incisor is about 1.0-1.5 mm;therefore, in the most severe of malalignment where two teeth wereliterally overlapping one another, channel widths of between 3 and 6 mm,such as between 4.5 and 6 mm, would be accommodating. Protrusions 3 band 3 d can extend beyond protrusions 3 a and 3 c in the heightdimension H by an amount of, for example, 1 to 2 mm, such as 1 to 1.5mm. Overall depth of the channels 2 a-d as measured from the top of thesmaller protrusion (e.g., protrusion 3 a in FIG. 1) can be between 1.2and 2.6 mm, such as between 1.9 and 2.6 mm, with top and bottom channels2 a, 2 b generally having greater depth than left and right channels 2c, 2 d. The generally elongate, smoothly contoured form with channelsmay be maintained while any or all of the noted useful dimensions arevaried by plus or minus fifteen percent. Implements within thesedimensions will be adequate to accommodate almost any malalignment.However, a smaller implement 1 may have insufficient strength and bemore susceptible to premature cracking during use. Further, implementscan be developed with different sizes to accommodate patients withdifferent sized teeth. For example, implements having dimensions nearthe bottom of the recited range may be appropriate for women, children,and young adults whereas implements having dimensions near the top ofthe recited range may be more appropriate for men.

Referring now to FIG. 8, a second embodiment of the implement 101 isseen to have a generally elongate, smoothly curvatured, form including atop channel 102 across its length L. In this overhead view, it is seenthat top channel 102 is not in the middle of the width W of theimplement 101, but is structured between a lip side 109 and a tongueside 110 which has more mass than the lip side 109. The implement 101 ofthis embodiment is otherwise generally symmetrical in that there isanother channel, not seen, parallel to top channel 102 on the underside.Thus the view from the underside is substantially identical to FIG. 8.However, it should be understood that top channel 102 need not beexactly over the opposite channel, but rather could be slightly offsetbut still generally parallel while still preserving the massrelationship of the lip side 109 and tongue side 110—that is, the tongueside is larger. The generally elongate form of implement 101 may be saidto have an axis through its length L, and the two channels also may besaid to have axes (not illustrated) substantially parallel to theimplement axis. The channels and the implement as a whole may, however,be slightly curved, with the lip side 109 being on the convex side ofthe curve.

Some useful, non-limiting dimensions of implement 101 of this embodimentare: Overall length, and length of channel 102 and its undersidecounterpart, 14 mm; width at the tops of the channels, 4 mm, and widthof the implement at its center, 9 mm. The average front to back width ofan incisor is about 1.0-1.5 mm; therefore, in the most severe ofmalalignment where two teeth were literally overlapping one another, thechannels would be accommodating. The generally elongate, smoothlycontoured form with channels may be maintained while any or all of thenoted useful dimensions are varied by plus or minus fifteen percent.That is, the length may vary from 11.9 to 16.1 mm, the width may varyfrom 7.6 to 10.35 mm, and the depth of one or both channels may varyfrom 1.7 to 2.3 mm, for example. Implements within these dimensions willbe adequate to accommodate almost any malalignment, it being understoodthat the mass of the tongue side 110 will remain larger than the mass ofthe lip side 109.

FIGS. 9-10 depict a section through the front of a patient's mouth withimplement 1, 101 applied for working. A retainer 204 covers upper(maxillary) tooth 205. An attachment 208 adheres to lower (mandibular)tooth 207. Aligner 206 generally follows the contour of lower tooth 207without necessarily conforming to its surface. Implement 1, 101 isplaced between the upper and lower teeth—that is, between retainer 204and aligner 206, such that upper tooth (or teeth) 205 and lower tooth(or teeth) 207 engage with the channels 2 a-d, 102. The patient then“works” the implement by sliding his or her teeth along the archescreated by channels 2 a-d, 102. Working the implement 1, 101 between theteeth in this position places a downward force on the aligner 206,providing the necessary action to move aligner 206 approximately intothe position represented by dotted line 211. A cycle of action wouldconsist of compression and release, where the aligner 206 is in theposition indicated by dotted line 211 during compression. The cycles ofcompression and release are important because this is when theprescribed directional forces are created. The force may be exerted uponcompression or release, depending on the prescribed tooth movement. InFIGS. 9-10, the bevel 212 is designed to allow the aligner 206 to hangfrom it upon release and, in doing so, apply a specific directionalforce.

Implement 1, 101 can be arranged in a number of different orientationswhile in patient's mouth. Selection of the appropriate orientation islargely up to the patient and based on what fits or feels the best forthe patient. Considerations as to what is most effective may also play arole, but the feel or fit is of primary concern as a comfortable feelwill best ensure the patient works implement 1, 101 for the appropriateamount of time.

For example, looking first to the first embodiment, implement 1 can bearranged in the patient's mouth with top channel 2 a oriented upwardsuch that it engages upper tooth 205 and bottom channel 2 b orienteddownward such that it can engage lower tooth 207. Implement 1 could alsobe arranged in the exact opposite orientation, with bottom channel 2 boriented upward and engaging upper tooth 205 and top channel 2 aoriented downward and engaging lower tooth 207. Assuming top and bottomchannels 2 a, 2 b have approximately the same dimensions, as is the casein FIG. 1, each of these two orientations would produce essentially thesame effect and feeling for patient. However, if there are slightdifferences in the dimensions of top and bottom channels 2 a, 2 b, eachof these two orientations would produce a slightly different feel. Byway of another example, implement 1 can be arranged in the patient'smouth with left channel 2 c oriented upward such that it engages uppertooth 205 and right channel 2 d oriented downward to engage lower tooth207. The opposite orientation, with right channel 2 d oriented upward,is also possible. Again, assuming left and right channels 2 c, 2 d haveapproximately the same dimensions, as in FIG. 1, each of these twoorientations would produce the same feel for the patient. However,because left and right channels 2 c, 2 d generally have less depth thantop and bottom channels 2 a, 2 b, orienting implement 1 with top channel2 a or bottom channel 2 b engaging top tooth 207 would produce adifferent feel for patient than if right channel 2 d or left channel 2 cwere to engage top tooth 207. Particularly, if top and bottom teethengage the less deep left and right channels 2 c, 2 d, the incisors (orother teeth engaging the implement 1) would rest in a more open positiondue to the additional bulk of the implement 1 between the teeth. “Open”refers to the level of closure of the jaw, which, in this scenario, isdetermined by the thickness of material between the incisor teeth. In amore open position, the jaw-closing muscles (masseter, temporalis, andmedial pterygoid) are more relaxed; therefore, it may be desirable tomaintain a more open position. By including channels of varying depth,the patient is given more options to find the best fit for implement 1.Further, as mentioned above, due to the symmetry of implement 1,implement 1 can dissolve in a consistent manner while maintaining itscross-sectional architecture and, therefore, functionality.

With respect to the second embodiment, implement 101 can be arrangedwith the lip side 109 forward and the tongue side 110 oriented towardthe interior of the mouth. Patient can then engage top channel 102 withupper tooth 205 and bottom channel with lower tooth 207. Implement 101can also be flipped along its elongated axis such that top channel 102engages lower tooth 207.

The channels 2 a-d, 102 are important for the clear aligner therapy,particularly with respect to incisor and anterior alignment therapies.Because of the implement's contour and multiple dimensions in differentdirections, the patient is able to work the implement 1, 101 back andforth as well as in cycles of compression and release, according to hisor her specific alignments and relative misalignments. The channels 2a-d, 102 are adapted to seat between opposing teeth in the anterior orincisor areas. The channels 2 a-d, 102 can span the entire width ofimplement 1, 101, extending from one side to the other, and areimportant to its application in the anterior, or incisor area, of thearch, where anterior-posterior (front-to-back) width is minimal and itis difficult to maintain anything between the teeth. The incentive tobite on and chew the implement 1, 101 is enhanced by the enticing mintflavoring and the xylitol additive.

Further, the shape of protrusions 3 a-d, is also important to theapplication of implement 1. The protrusions 3 a-d assist in maintainingimplement 1 in place between the teeth while it is worked back and forthby acting as a barrier that prevents the tooth from slipping out of thearch of channel 2 a-d. The shape of protrusions 3 a-d should furtherthis purpose but one should not create intrusive bulk or cumbersomemobility within the mouth while working implement 1 along the arch. Inuse, the smaller protrusions 3 a, 3 c, are generally positioned on thetongue side of the lower teeth because the anterior teeth are not smoothall the way to the gum line like as is the case on the lip side of theanterior teeth due to the cingulum on each tooth.

The implement 1, 101 is constructed to provide resiliency sufficient forthe implement to maintain its shape after repeated chewing and workingin the seat between opposing teeth. It will break down after varyingtime periods, depending on two kinds of variables, namely those relatingto the structure and composition of the implement, and those determinedby the vagaries of chewing force, frequency of cycles, and compositionof the patient's saliva. Although I do not intend to be bound to anyparticular longevity for a single implement, a useful duration period isthree to five minutes of chewing and working (continued action), duringwhich the flavoring and the xylitol are released. The implement may havea hard but chewable coating to assure that its shape will be maintainedover a desired period of time.

It should be understood that the multi-concave nature of implement 1,101, characterized by opposing grooves or channels, provides a quicklyunderstood incentive for the patient to place it between his or herteeth and work it. The therapeutic aspects of the implement are not onlyreadily adopted, but the implement is easy to maintain in the properposition, thereby encouraging its use. The benefits or motivations forusing any auxiliary implement are important in understanding thelikelihood of compliance. For example, a few of the possible benefits ormotivations for using implement with aligner therapy are the following:

-   -   The implement makes aligner therapy more enjoyable.    -   The implement improves the efficiency of aligner therapy.    -   Because the aligner therapy is more efficient, treatment times        are reduced, which is beneficial to both the patient and the        provider.    -   Clinical outcomes are improved.    -   Discomfort associated with aligner therapy is alleviated.    -   Greater patient satisfaction with aligner therapy benefits the        provider as well as the patient.    -   Because of increased efficiency of treatment, costs are reduced.    -   The implement facilitates the integration of aligner therapy        into the everyday lifestyle of the patient. Use of implement may        be quite discreet compared to prior art therapies which require        conspicuously grasping a handle or stem by hand to keep a        chewing device in place.

Chewies™, through experience, do not make aligner therapy more enjoyablemainly due to their need to be cleaned and re-used, as well as theadditional hand that is needed to keep one in place throughout its use.Furthermore, requiring the use of Chewies™ does not improve theintegration of aligner therapy into everyday life. Acceledent® has beenreported to be easier to integrate into treatment due to its extremelyhigh frequency of vibration and therefore only twenty minutes per dayusage. However, it vastly increases costs for both the clinician andpatient. All of the above benefits and advantages are present in myinvention, which, in addition, is simple and inexpensive.

The implement's composition and construction are preferably intended toallow both the flavoring and the coherent mass to last for approximately3-5 minutes. The minimum recommended protocol for usage of eachimplement is to apply two implements, one after the other in sequence,for approximately 3-5 minutes each, following the insertion of analigner. To “apply” the implement means to work (gently chew) one ormore implement(s) in succession around the dentition for approximately3-5 minutes following the insertion of an aligner. This will ensure thateach time the aligners are taken out, presumably to eat and/or brush,and placed back in the mouth, they are given the proper action that isrequired to achieve desired results. Continued usage (continued action)of the implements throughout treatment, above and beyond the minimumrecommended protocol, can shorten treatment time an estimated 15-25%(currently based on empirical evidence and clinical experience).

Notwithstanding the utility of an implement having a longevity of 3-5minutes under gentle chewing as described above, the durability of asingle implement is not important to accomplish the goals of bothbreath-freshening and superior functionality. Rather, it is mostimportant that the patient apply continued action for a daily total ofat least 30 minutes.

The implement is consumable, meaning that it may be swallowed and isdigestible. Desirable ingredients for making a consumable mass includemagnesium stearate as a filling agent, one or more flavoring extracts,such as mint, xylitol, preferably with calcium lactate as a carrier, gumarabic as a binding agent, and camuba wax for a hard crust or shell.Sodium CMC, or cellulose gum, may also be used as a binder or filler.All of these ingredients may be swallowed and digested. Ingredients andmethods used to make a consumable mass suitable for the presentinvention are generally known in the art, such as in U.S. Pat. No.8,431,150 to Stawski et al., U.S. Pat. No. 6,582,731 to Kaufmann, andU.S. Pat. No. 6,083,527 to Thistle, each of which is herein incorporatedby reference.

Generally, the proportions of the ingredients are selected so that theimplement may be worked for at least three minutes without breaking up;however, a particular life span of a single implement is not criticalfor the therapy, which is designed around a prescribed daily performanceof continued action. The number of implements consumed in a day is notas important as a range of cycles of continued action. The patient mayprefer to work implement for only a minute or less; this is satisfactoryso long as the number of implements per day is increased accordingly.

Thus, described is an orthodontic aligner implement comprising aconsumable mass including channels on opposite sides and traversing thewidth of the mass, the channels being adapted to seat between opposinganterior or incisor teeth. Also described is a method of positioning anorthodontic aligner into a prescribed position comprising (a) placingthe aligner approximately in the prescribed position in one's mouth, (b)placing an aligner implement into the mouth, and (c) applying saidimplement in contact with the aligner in one's mouth. It also includes amethod of promoting the acceleration of tooth movement in a patientundergoing clear aligner therapy comprising prescribing for the patienta regimen including successively applying a plurality of alignerimplements of between the upper and lower teeth soon after eachplacement of the aligner implement in the mouth, for a total of at least30 minutes in a day.

Although the invention has been described in detail for the purpose ofillustration based on what is currently considered to be the mostpractical and preferred embodiments, it is to be understood that suchdetail is solely for that purpose and that the invention is not limitedto the disclosed embodiments, but, on the contrary, is intended to covermodifications and equivalent arrangements. For example, it is to beunderstood that the present invention contemplates that, to the extentpossible, one or more features of any embodiment can be combined withone or more features of any other embodiment.

The invention claimed is:
 1. A method of positioning an orthodonticaligner into a prescribed position comprising: (a) placing said alignerat least approximately in the prescribed position in one's mouth; (b)placing an aligner implement into the mouth, wherein the alignerimplement comprises a consumable mass having a top side and a bottomside opposite the top side, wherein each of the top side and the bottomside includes a single channel traversing the width of said mass, saidchannels being adapted to seat between opposing anterior or incisorteeth; (c) positioning the aligner implement such that opposing anterioror incisor teeth are seated within said channels; and (d) with saidimplement positioned as in step (c), applying pressure between saidimplement and said aligner.
 2. The method of claim 1 comprisingperforming the applying of step (d) for at least three minutes.
 3. Themethod of claim 1 further comprising repeating steps (b), (c), and (d)with a second aligner implement, wherein the second aligner implementcomprises a consumable mass having a top side and a bottom side oppositethe top side, wherein each of the top side and the bottom side includesa single channel traversing the width of said mass, said channels beingadapted to seat between opposing anterior or incisor teeth.
 4. Themethod of claim 1 wherein said applying is performed for 3-5 minutes. 5.The method of claim 1 further comprising repeating steps (b), (c), and(d) with one or more additional aligner implements, wherein each of theone or more additional aligner implements comprises a consumable masshaving a top side and a bottom side opposite the top side, wherein eachof the top side and the bottom side includes a single channel traversingthe width of said mass, said channels being adapted to seat betweenopposing anterior or incisor teeth, so that the total contact timebetween said aligner implements and said aligner is at least 30 minutesin a day.
 6. A method of promoting the acceleration of tooth movement ina patient undergoing clear aligner therapy comprising prescribing forsaid patient a regimen including: a) placing an aligner at leastapproximately in a prescribed position in the patient's mouth; (b)placing an aligner implement into the patient's mouth, wherein thealigner implement comprises a consumable mass having a top side and abottom side opposite the top side, wherein each of the top side and thebottom side includes a single channel traversing the width of said mass,said channels being adapted to seat between opposing anterior or incisorteeth; (c) positioning the aligner implement such that opposing anterioror incisor teeth are seated within said channels; and (d) with saidimplement positioned as in step (c), applying pressure between saidimplement and said aligner.
 7. The method of claim 6 wherein saidaligner implement includes at least 0.5 grams of a sweetener whichcannot be metabolized by oral bacteria.
 8. The method of claim 7 whereinsaid sweetener is xylitol.
 9. The method of claim 6 wherein said alignerimplement includes mint flavoring in an, amount sufficient to last atleast three minutes while pressure is being applied in step (d).